A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17584073



Internal ID21776116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47759297..47759297hg38UCSC Ensembl
chr10:46967091..46967091hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6096811
Supporting Variants
Samples
Known GenesSYT15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17584073
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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